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483 Frontida BioPharm, Jul 2019

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FDA investigators audited the Frontida BioPharm - Philadelphia , PA, United States facility and issued inspectional observation (via FDA 483) on 19 Jul 2019.

Product Details

  • Inspection end: 19 Jul 2019
  • Location: Philadelphia, United States
  • FEI: 2523348
Frontida BioPharm FDA inspection 483 Jul 2019

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